美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
68071-4760-3	68071-4760	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190208	N/A	ANDA	ANDA090162	NuCare Pharmaceuticals,Inc.	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4760-3)
71335-1064-0	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1064-0)
71335-1064-1	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1064-1)
71335-1064-2	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190111	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1064-2)
71335-1064-3	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190115	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1064-3)
71335-1064-4	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1064-4)
71335-1064-5	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190131	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1064-5)
71335-1064-6	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	80 TABLET, FILM COATED in 1 BOTTLE (71335-1064-6)
71335-1064-7	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1064-7)
71335-1064-8	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-1064-8)
71335-1064-9	71335-1064	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090162	Bryant Ranch Prepack	TOPIRAMATE	50 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1064-9)
83008-011-30	83008-011	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230324	20260831	ANDA	ANDA090162	Quality Care Products, LLC	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (83008-011-30)
83008-012-60	83008-012	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230509	20260331	ANDA	ANDA090162	Quality Care Products, LLC	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (83008-012-60)